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Clinical Contracts Associate Jobs in Texas (NOW HIRING)

Tekhawks LLC

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Sr. Clinical Contracts Associate - Plano, TX or Maple Grove, MN

Plano, TX · On-site

$45 - $55/hr

Job Title: Sr. Clinical Contracts Associate Duration: 12+ Months Location: Plano, TX or Maple Grove, MN Position Overview Seeking a Clinical Contracts Associate to support the development ...

Tekhawks LLC

Be Seen First

Sr. Clinical Contracts Associate - Plano, TX or Maple Grove, MN

Plano, TX · On-site

$45 - $55/hr

Job Title: Sr. Clinical Contracts Associate Duration: 12+ Months Location: Plano, TX or Maple Grove, MN Position Overview Seeking a Clinical Contracts Associate to support the development ...

Abbott

Clinical Contracts Associate II

Plano, TX

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as preferred location. This is an in-office position Position Summary Working under the direction of ...

Abbott

Clinical Contracts Associate II

Plano, TX

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as preferred location. This is an in-office position Position Summary Working under the direction of ...

Abbott

Clinical Site Lead - Dallas, TX

Dallas, TX · On-site

The Clinical Site Lead drives study execution and operational excellence across Abbott ... Site CRA, Site Contract Associate. Train facility staff regarding protocol requirements and ...

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Clinical Contracts Associate information

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$14

$33

$51

How much do clinical contracts associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical contracts associate in Texas is $33.86, according to ZipRecruiter salary data. Most workers in this role earn between $24.62 and $40.77 per hour, depending on experience, location, and employer.

What is a clinical contracts associate?

Clinical Contracts Associates are professionals who manage and negotiate contracts related to clinical trials and research studies, typically within the pharmaceutical, biotechnology, or healthcare industries. They ensure that agreements with research sites, vendors, and other stakeholders are compliant with legal, regulatory, and company requirements. Their responsibilities often include drafting, reviewing, and revising contracts, as well as collaborating with legal, finance, and clinical operations teams. Clinical Contracts Associates play a crucial role in supporting the timely initiation and execution of clinical studies.

What are some common challenges a clinical contracts associate faces when negotiating agreements with clinical trial sites?

Clinical Contracts Associates often encounter challenges such as balancing sponsor requirements with site preferences, addressing complex regulatory and compliance issues, and ensuring contract language aligns with both parties' expectations. Negotiations may be prolonged due to differences in legal terms, indemnification, or budget concerns. Effective communication, attention to detail, and the ability to prioritize multiple agreements simultaneously are essential for overcoming these obstacles and maintaining positive relationships with sites.

What are the key skills and qualifications needed to thrive as a clinical contracts associate, and why are they important?

A Clinical Contracts Associate should possess strong knowledge of contract law, clinical trial processes, and regulatory compliance, typically supported by a bachelor's degree in life sciences, business, or a related field. Familiarity with contract management systems, Microsoft Office Suite, and eClinical tools is commonly required, and certifications such as CCRA or similar are advantageous. Excellent negotiation, attention to detail, and effective communication skills help manage stakeholder expectations and resolve issues efficiently. These skills are crucial for ensuring timely, compliant contract execution and supporting the smooth operation of clinical research projects.

What is the difference between Clinical Contracts Associate vs Clinical Research Coordinator?

AspectClinical Contracts Associate
Primary RoleDrafting, reviewing, and negotiating clinical trial contracts and budgets
Required SkillsLegal knowledge, contract management, attention to detail
Work EnvironmentCorporate or sponsor offices, legal or contracts departments
Common CertificationsNone specifically required, but legal or contract management certifications are a plus

The Clinical Contracts Associate primarily focuses on managing and negotiating contracts related to clinical trials, ensuring compliance and proper budgeting. In contrast, a Clinical Research Coordinator handles the day-to-day operations of clinical trials, including patient recruitment and data collection. Both roles are essential in the clinical research industry but serve different functions within the trial process.

What are the most commonly searched types of Clinical Contracts jobs in Texas?

The most popular types of Clinical Contracts jobs in Texas are:

What cities in Texas are hiring for Clinical Contracts Associate jobs?

Cities in Texas with the most Clinical Contracts Associate job openings:

Clinical Contracts Associate jobs near you

Sr. Clinical Contracts Associate - Plano, TX or Maple Grove, MN

Tekhawks LLC

Plano, TX • On-site

$45 - $55/hr

Contractor

Posted 5 days ago

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Job description

Job Title: Sr. Clinical Contracts Associate

Duration: 12+ Months
Location: Plano, TX or Maple Grove, MN

Position Overview
Seeking a Clinical Contracts Associate to support the development, negotiation, review, and execution of clinical study contracts and site budgets. The consultant will work directly with clinical sites and internal stakeholders to resolve contracting and budget issues and support study timelines.
Responsibilities

  • Develop and negotiate clinical site contracts, amendments, and budgets.
  • Manage routine contract negotiations with limited supervision.
  • Partner with internal and external stakeholders to resolve contracting and budget issues.
  • Review informed consent documents for alignment with contract terms.
  • Identify potential contract, budget, and compliance risks and support timely resolution.
  • Ensure contracting activities meet study timelines and established metrics.


Requirements

  • Associate’s degree or equivalent with 5+ years of related experience.
  • Knowledge of contract law, legal terminology, and clinical contracting principles.
  • Familiarity with GCP, ICH, GLP, and regulations governing clinical grants and contracts.
  • Understanding of Sunshine Act, FWA, Human Subject Protection, and clinical insurance requirements.
  • Strong negotiation, organizational, analytical, and communication skills.
  • Proficiency with Microsoft Word and Excel.
  • Sponsor-side pharma or biotech contracting experience preferred.
  • Clinical site budgeting and document redlining experience preferred.